Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jun-fei Yi"'
Autor:
Jun Fu, Yi-Ming Zheng, Su-Qin Jin, Jun-Fei Yi, Xiu-Juan Liu, He Lyn, Zhao-Xia Wang, Wei Zhang, Jiang-Xi Xiao, Yun Yuan
Publikováno v:
Chinese Medical Journal, Vol 129, Iss 15, Pp 1811-1816 (2016)
Background: Collagen VI-related myopathies are autosomal dominant and recessive hereditary myopathies, mainly including Ullrich congenital muscular dystrophy (UCMD) and Bethlem myopathy (BM). Muscle magnetic resonance imaging (MRI) has been widely us
Externí odkaz:
https://doaj.org/article/54371d459af04903a8eb286703eb59bd
Publikováno v:
BMC Musculoskeletal Disorders, Vol 24, Iss 1, Pp 1-12 (2023)
Abstract Background The aging of the population is a social problem faced by many countries in the world. With the increase in the elderly population, the number of patients with Kummell’s disease is also gradually increasing. No study has demonstr
Externí odkaz:
https://doaj.org/article/aa3429532e204c75bbbf92b3b2da6bbf
Objective: To investigate the outcome of modified anterior cervical corpectomy and fusion(mACCF) without corpectomy C4 or C5 vertebral body in the treatment of four-level cervical spondylotic myelopathy (CSM). Methods: 34 consecutive patients suffere
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e403cf3ad49514bb259a18f8d5e887a
https://doi.org/10.21203/rs.3.rs-2259144/v1
https://doi.org/10.21203/rs.3.rs-2259144/v1
BackgroundThe aging of the population is a social problem faced by many countries in the world. With the increase in the elderly population, the number of patients with Kummell’s disease is also gradually increasing. No study has demonstrated that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5db2c21c366e8df051667be4e1c32256
https://doi.org/10.21203/rs.3.rs-1882800/v1
https://doi.org/10.21203/rs.3.rs-1882800/v1
Publikováno v:
Journal of human genetics. 63(10)
Large deletions and duplications are the most frequent causative mutations in Becker muscular dystrophy (BMD), but genetic profile varied greatly among reports. We performed a comprehensive molecular investigation in 95 Chinese BMD patients. All pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d384928022286b8bed3c8e9f36eab5ee
https://pubmed.ncbi.nlm.nih.gov/29976999
https://pubmed.ncbi.nlm.nih.gov/29976999